Transition-State Structure of - American Chemical Society

Oct 23, 2007 - Received July 20, 2007; E-mail: [email protected]. 5′-Methylthioadenosine/S-adenosylhomocysteine nucleosidase. (MTAN) is a bacterial ...
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Transition-State Structure of Neisseria meningitides 5′-Methylthioadenosine/ S-Adenosylhomocysteine Nucleosidase Vipender Singh,† Minkui Luo,† Rosemary L. Brown,‡ Gillian E. Norris,‡ and Vern L. Schramm*,† Department of Biochemistry, Albert Einstein College of Medicine, 1300 Morris Park AVenue, Bronx, New York 10461, and Institute of Molecular Biosciences, Massey UniVersity, PriVate Bag 11222, Palmerston North, New Zealand Received July 20, 2007; E-mail: [email protected]

5′-Methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) is a bacterial enzyme of the N-ribosyltransferase family. It catalyzes the biologically irreversible hydrolytic deadenylation of 5′-methylthioadenosine (MTA) or S-adenosylhomocysteine to form adenine and methylthioribose (MTR) or S-ribosylhomocysteine, respectively (Figure 1). MTAN is involved in bacterial quorum sensing pathways and thus is a potential target for the design of antibiotics.1-4 There is no MTAN in humans, where 5′methylthioadenosine phosphorylase (MTAP) catalyzes the reversible phosphorolysis of MTA to adenine and methylthioribose-1phosphate. MTAP has been targeted in the design of anticancer drugs on the basis of its involvement in polyamine biosynthesis and purine salvage pathways.5-6 Probing transition-state structures of these enzymatic reactions provides an approach for the design of transition-state analogues as powerful inhibitors. This strategy has been successfully applied in the development of inhibitors for E. coli and S. pneumoniae MTANs with dissociation constants to the femtomolar range.7,8 Here we report that Neisseria meningitides MTAN forms a transition state unique from other MTANs. This surprising result adds another example of closely related enzymes with distinct transition-state structures.9-12 Transition-state analogues of bacterial quorum sensing pathways have potential for blocking virulence gene expression without affecting growth, thus minimizing the probability of generating bacterial strains resistant to quorum-sensing antibiotics. The transition states of E. coli and S. pneumoniae MTANs were recently solved using kinetic isotope effects (KIE).10,11 They were shown to have dissociative SN1 transition states with little or no bond order to the leaving adenine or to the attacking hydroxyl nucleophile. However, a key distinction between these two transition states is the protonation state of adenine N7 at the transition state. In E. coli MTAN, N7 is protonated to give a neutral leaving group. The N7 of adenine is not protonated at the transition state of S. pneumoniae MTAN, creating a relatively unfavorable anionic leaving group. This feature differentiates S. pneumoniae and E. coli MTAN transition states and explains why E. coli MTAN is catalytically ∼103-fold more efficient than S. pneumoniae MTAN. The transition state of human MTAP also exhibits significant dissociative character in which the N-glycosidic bond is fully broken and the leaving group adenine is anionic.13 However, a unique feature of human MTAP in comparison with E. coli and S. pneumoniae MTANs is that human MTAP involves significant participation of the phosphate nucleophile. The properties of ribose sugars at the transition states of E. coli and S. pneumoniae MTANs and human MTAP also make these enzymes different from other enzymes of the N-ribosyltransferase family. The transition states of human and Plasmodium falciparum † ‡

Albert Einstein College of Medicine. Massey University.

10.1021/ja0754204 CCC: $37.00 © 2007 American Chemical Society

Figure 1. Hydrolysis of MTA by N. meningitides MTAN and the proposed transition-state structure. Cationic features of the transition state are indicated in blue.

purine nucleoside phosphorylases (PNPs) are fully dissociated ribocations while that for bovine PNP is an early SN1 transition state.9,14 In contrast, the transition states of MTANs from E. coli and S. pneumoniae and human MTAP appear to be zwitterionic, cationic at the anomeric carbon, and anionic at the 3′-hydroxyl oxygen. The transition state of bovine PNP differs from other PNPs in that the nucleoside reactant retains substantial bond order to the hypoxanthine leaving group. This difference in transition-state structure occurs despite the 87% sequence identity between bovine and human PNPs and their completely conserved catalytic sites.9,14,15 This surprising variety in the N-ribosyltransferase transition states led to the present analysis of the MTAN from N. meningitides. All previously reported MTAN transition states are characterized by fully dissociated leaving groups with no participation of the water nucleophile. However, associative transition states are found in other enzymes of the N-ribosyltransferase family, and we explored this possibility for a family of MTANs. We screened several MTANs with MT-Immucillin-A, a transition-state analogue of early SN1 transition states for MTANs, in comparison to inhibition by MTDADMe-Immucillin-A, an analogue of fully dissociated transition states.7-11 N. meningitides MTAN gave an inhibition profile suggesting an early transition state. Catalytic turnover of N. meningitides MTAN (kcat ) 8 s-1) is similar to that of E. coli MTAN (kcat ) 3 s-1).16 Kinetic isotope effect analysis and computational modeling were used to solve the transition-state structure of N. meningitides MTAN. The study establishes that the N. meningitides MTAN has an early SN1 transition state with significant N-glycosidic bond order at the transition state. The early transition state of N. meningitides MTAN is consistent with its inhibition by transition-state analogues of MTANs.16 The N. meningitides MTAN is the first reported MTA hydrolase to have an early transition state with significant bond order to the adenine leaving group. The transition state of N. meningitides MTAN was probed with pairs of isotopically labeled MTAs, synthesized enzymatically.10 Experimental KIEs were measured for MTAs labeled at [1′-3H], J. AM. CHEM. SOC. 2007, 129, 13831-13833

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Figure 2. Intrinsic and calculated KIEs (left) and the modeled transition state (right) of N. meningitides MTAN. The MEP model shown top on the right was calculated at HF/STO3G (Gaussian 98/cube) for the geometry optimized at the B3LYP/6-31G(d,p) level of theory and visualized with Molekel 4.020 at density of 0.15 electrons/Å3. The stick model shown below on the right has the same geometry as the MEP surface, and the bond length is in Å.

[1′-14C], [2′-3H], [4′-3H], [5′-3H2], [9-15N] and [Me-3H3]. Experimental KIEs were measured for MTAs under competitive conditions known to give KIEs with kcat/Km (V/K) kinetic parameters.17 KIEs were measured by comparing the 3H/14C ratio in products formed from each pair of isotopically labeled MTAs (Supporting Information).10 [5′-14C]MTA was used as the isotopically silent remote label to examine the 3H isotope effects and both [4′-3H]- and [5′-3H2] MTAs were used as the remote labels for measuring [1′-14C] and [9-15N, 5′-14C] KIEs. The [1′-14C] and [9-15N, 5′-14C] KIEs were subsequently corrected for the remote [3H] KIE. All KIEs were corrected to represent the isotope effects extrapolated to 0% hydrolysis according to the equation

KIE )

ln(1 - f ) Rf ln 1 - f Ro

[(

)]

where f is the fraction of reaction progress, Rf and Ro are ratios of heavy to light isotope at partial and total reaction completion, respectively. The V/K KIEs obtained above were further corrected for forward commitment using Northorp’s equation modified for irreversible reaction: H(V/K) ) (Hk + Cf)/(1 + Cf), where H(V/K) is the observed heavy atom isotope effect measured experimentally, Cf is the forward commitment to catalysis, and Hk is the intrinsic isotope effect.17 The forward commitment to catalysis was measured using the isotope partition method as described previously for E. coli MTAN.10,18 MTAN from N. meningitides exhibits a relatively large forward commitment factor of 0.66 ( 0.027 (Supporting Information), consistent with its small Km of 1.4 µM.16 The V/K KIEs were corrected for forward commitment to obtain the intrinsic KIEs for [1′-3H]-, [1′-14C]-, [2′-3H]-, [4′-3H]-, [9-15N]-, [5′-3H2]-, and [Me-3H3] MTAs (Figure 2). Intrinsic KIEs were used as constraints to match a transitionstate structure of N. meningitides MTAN calculated with B3LYP functional density theory and the 6-31G(d,p) basis set implemented in Gaussian 98 or Gaussian 03.19 Transition-state optimization for N. meningitides was initiated by making small perturbations to the C1′-N9 bond of MTA. The KIEs were calculated for each perturbation and compared to the intrinsic KIEs. The transitionstate optimization process was completed when the calculated isotope effects were closely matched to the intrinsic KIEs (Figure 2). 13832 J. AM. CHEM. SOC.

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The calculated transition state for hydrolysis of MTA by N. meningitides MTAN shows good agreement with the intrinsic KIEs. At the transition state the C1′-N9 glycosidic bond is weakened with an increase in bond length from 1.47 Å for MTA to 1.68 Å. This bond length corresponds to a Pauling bond order of 0.50, the earliest transition state known for any dissociative N-ribosyltransferase, since others have C1′-N9 bond orders of 0.38 to